Last reviewed · How we verify

HRZE

Global Alliance for TB Drug Development · Phase 3 active Small molecule

HRZE is a fixed-dose combination of four first-line anti-tuberculosis drugs that work synergistically to inhibit bacterial cell wall synthesis and mycolic acid production.

HRZE is a fixed-dose combination of four first-line anti-tuberculosis drugs that work synergistically to inhibit bacterial cell wall synthesis and mycolic acid production. Used for Tuberculosis (drug-susceptible, pulmonary and extrapulmonary).

At a glance

Generic nameHRZE
Also known asINH, RMP, PZA and EMB, isoniazid, H, rifampicin, R
SponsorGlobal Alliance for TB Drug Development
Drug classFixed-dose combination antituberculous agent
TargetMultiple: KatG/InhA (isoniazid), bacterial RNA polymerase (rifampicin), PncA/RpoB (pyrazinamide), arabinosyl transferase (ethambutol)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhasePhase 3

Mechanism of action

HRZE combines isoniazid (INH), rifampicin (RIF), pyrazinamide (PZA), and ethambutol (EMB), each targeting different aspects of Mycobacterium tuberculosis metabolism and cell wall integrity. Isoniazid inhibits mycolic acid synthesis, rifampicin blocks RNA polymerase, pyrazinamide disrupts energy metabolism in acidic environments, and ethambutol inhibits arabinosyl transferases. The combination provides rapid bactericidal activity and reduces the emergence of drug-resistant strains.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results